SBIR/STTR Research Award

Stabilization Device for Transseptal Access

Award identifier a1d5bd60f94928833daa15ed2c4d2277029f6c931d942526b0206465beee8d39Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$154,800

Program and phase

SBIR · Phase I

Award year

2013

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
PACIFIC SCIENCE & ENGINEERING GROUP, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
JNJDX2LYQ9L9
Solicitation number
PA12-088
Topic code
NINR

Research abstract

DESCRIPTION (provided by applicant): The goal of this project is to design a new type of bedside incentive spirometer to help minimize respiratory complications, such as pneumonia and atelectasis, among postoperative patients. The bedside incentive spirometers in current widespread use in hospitals have several severe shortcomings, including inadequate patient feedback, no reminder mechanism to prompt their use by patients, and no means for physicians and nurses to assess patient breathing performance andtreatment compliance. In this project, we will design a digital interactive bedside incentive spirometer, based on physician, nurse, and patient input, which avoids these drawbacks by incorporating an enhanced feature set and user interface design. Our central hypothesis is that our new incentive spirometer will improve patient breathing performance and treatment compliance and be more informative and useful to physicians and nurses, compared with current bedside incentive spirometers. The rationale for this project is that greater patient compliance will reduce postoperative respiratory complications, shorten the duration of postoperative hospitalization, and minimize the need for rehospitalization for respiratory compromise, all of which enhance patient welfare and reduce healthcare costs. We will accomplish project objectives by addressing three specific aims: 1) To develop design specifications for a prototype incentive spirometer. This prototype spirometer will be easy for patients to learn, use, and understand, while enabling physicians and nurses to accurately assess patient breathing performance, adherence to prescribed treatment, and breathing performance trends over time. The applied science of human factors engineering will be used to define user needs and requirements and to develop prototype design concepts and specifications. 2) To evaluate the ease of use of the prototype spirometer by constructing several low-fidelity prototype models and assessing their feature sets and interface designs so that areas of improvement can be identified. Healthcare providers will play a vital role in the design and test process by identifying needed healthcare features and evaluating prototype interface design. 3) Based on the results of the usability evaluations,we will refine the design specifications of the prototype spirometer to maximize its effectiveness and ease of use. The outcome of this effort will be a detailed and tested design specification and a prototype spirometer that is based on human factors engineering principles and physician, nurse, and patient input. This prototype device will significantly improve patient breathing performance and treatment adherence relative to incentive spirometers in current widespread use. It will also enable physicians and nurses to directly assess patients' breathing performance and adherence. This new spirometer is expected to have an important positive impact on patients' well-being by reducing the incidence and severity of postoperative respiratory complications. Given the widespread use of incentive spirometry among postoperative patients, the commercial potential and impact on patient outcome of this device is significant. PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: We will design a new type of bedside incentive spirometer with features that will encourage greater patient treatment compliance compared with the bedside incentive spirometers currently in widespread use. This new device will also allow physicians and nurses to more reliably monitor patient breathing performance, compliance with device use, and respiratory trends over time. Its benefits are expected to include fewer postoperative respiratory complications, shorter postoperative hospitalization, and fewer respiratory-related rehospitalizations.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

56 SBIR/STTR records share this UEI (1990–2025). Reported award amounts total $30,109,713. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Defense, Department of Energy, Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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